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白细胞介素-1 受体样 1 多态性与儿童血清 IL1RL1-a、嗜酸性粒细胞和哮喘有关。

Interleukin-1 receptor-like 1 polymorphisms are associated with serum IL1RL1-a, eosinophils, and asthma in childhood.

机构信息

Departments of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

出版信息

J Allergy Clin Immunol. 2011 Mar;127(3):750-6.e1-5. doi: 10.1016/j.jaci.2010.12.014. Epub 2011 Feb 1.

Abstract

BACKGROUND

IL-1 receptor-like 1 (IL1RL1) is a membrane receptor involved in T(H)2 inflammatory responses and eosinophilia. Single nucleotide polymorphisms (SNPs) in IL1RL1 have been associated with blood eosinophil counts in a genome-wide association study and with asthma in family-based and case-control studies.

OBJECTIVE

We assessed in the prospective birth cohort Prevention and Incidence of Asthma and Mite Allergy (PIAMA) whether IL1RL1 SNPs associate with levels of its soluble transcript IL1RL1 (IL1RL1-a) in serum, blood eosinophil counts, and asthma prevalence from birth to age 8 years, and whether IL1RL1-a serum levels associate with blood eosinophil counts.

METHODS

Fifteen IL1RL1 SNPs were genotyped. Serum IL1RL1-a levels were measured in 2 independent subsets within PIAMA, at 4 and 8 years. Blood eosinophil counts were measured in 4-year-old children.

RESULTS

In 2 independent subsets of children, 13 of 15 SNPs were associated with serum IL1RL1-a levels at ages 4 and 8 years with a consistent direction of effect for each allele. Rs11685480 allele A and rs1420102 allele A were significantly associated with lower numbers of blood eosinophils. In the total cohort, rs1041973 allele A was associated with a decreased risk of developing asthma (odds ratio, 0.70; 95% CI, 0.54-0.90). Rs1420101, recently identified in a genome-wide association study in the Icelandic population, was not associated with asthma in this study. IL1RL1-a levels were not associated with eosinophil counts.

CONCLUSION

We demonstrate that IL1RL1 polymorphisms are associated with serum IL1RL1-a, blood eosinophils, and asthma in childhood.

摘要

背景

白细胞介素 1 受体样 1(IL-1RL1)是一种参与 T(H)2 炎症反应和嗜酸性粒细胞增多的膜受体。全基因组关联研究发现,IL-1RL1 中的单核苷酸多态性(SNP)与血液嗜酸性粒细胞计数有关,家族性和病例对照研究发现与哮喘有关。

目的

我们在前瞻性出生队列预防和哮喘及螨变应性研究(PIAMA)中评估,IL-1RL1 SNP 是否与血清可溶性转录物 IL-1RL1(IL-1RL1-a)水平、血液嗜酸性粒细胞计数以及从出生到 8 岁的哮喘患病率相关,以及 IL-1RL1-a 血清水平是否与血液嗜酸性粒细胞计数相关。

方法

共检测了 15 个 IL-1RL1 SNP。在 PIAMA 中,2 个独立的亚组分别在 4 岁和 8 岁时测量了血清 IL-1RL1-a 水平。在 4 岁的儿童中测量了血液嗜酸性粒细胞计数。

结果

在 2 个独立的儿童亚组中,15 个 SNP 中有 13 个与 4 岁和 8 岁时的血清 IL-1RL1-a 水平相关,每个等位基因的效应方向一致。rs11685480 等位基因 A 和 rs1420102 等位基因 A 与较低的血液嗜酸性粒细胞计数显著相关。在整个队列中,rs1041973 等位基因 A 与哮喘发病风险降低相关(比值比,0.70;95%CI,0.54-0.90)。最近在冰岛人群全基因组关联研究中发现的 rs1420101 在本研究中与哮喘无关。IL-1RL1-a 水平与嗜酸性粒细胞计数无关。

结论

我们证明 IL-1RL1 多态性与儿童时期的血清 IL-1RL1-a、血液嗜酸性粒细胞计数和哮喘有关。

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